Cytotoxic T lymphocytes recognize a fragment of influenza virus matrix protein in association with HLA-A2 (original) (raw)
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- Published: 01 April 1987
Nature volume 326, pages 881–882 (1987)Cite this article
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Abstract
Both human and murine cytotoxic T cells (CTL) elicited in response to infection with influenza A viruses have been shown to be specific for internal viral proteins, such as the matrix and nucleoprotein1–3. Individual CTL epitopes have been identified in the nucleoprotein by successfully substituting short synthetic peptides for the intact virus in the preparation of target cells in cytotoxicity assays4. The defined peptide epitopes have each been recognized by CTL in association with individual class I major histocompatibility complex (MHC) proteins, H–2Db (ref. 4), H–2Kk (ref. 5), H–2Kd (Taylor, P. et al., unpublished data) and HLA-B37 (refs 4,6). A logical strategy to investigate the molecular details of the interaction between antigen and MHC class I proteins would be to define an epitope recognized by the MHC class I molecule HLA-A2. This is because the amino-acid sequence is known, several variants of A2 have been characterized and the protein has been purified and crystallized7–11. Here we describe a peptide derived from the influenza matrix protein that is recognized by human CTL in association with the HLA-A2 molecule.
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Authors and Affiliations
- Nuffield Department of Medicine, John Radcliffe Hospital, Headington, Oxford, OX3 9DU, UK
Frances Gotch, Alain Townsend & Andrew McMichael - Imperial Cancer Research Fund Laboratories, Lincoln's Inn Fields, London, WC1, UK
Jonathan Rothbard & Kevin Howland
Authors
- Frances Gotch
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You can also search for this author inPubMed Google Scholar - Kevin Howland
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Gotch, F., Rothbard, J., Howland, K. et al. Cytotoxic T lymphocytes recognize a fragment of influenza virus matrix protein in association with HLA-A2.Nature 326, 881–882 (1987). https://doi.org/10.1038/326881a0
- Received: 16 February 1986
- Accepted: 20 March 1986
- Published: 01 April 1987
- Issue Date: 30 April 1987
- DOI: https://doi.org/10.1038/326881a0